"DGH" Keratoscope (Non-Sterile) - Taiwan Registration 91c4a39e81030c3999a2eefb445bdff7
Access comprehensive regulatory information for "DGH" Keratoscope (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 91c4a39e81030c3999a2eefb445bdff7 and manufactured by DGH Technology Inc.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DGH Technology Inc., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
91c4a39e81030c3999a2eefb445bdff7
Ministry of Health Medical Device Import No. 017752
DHA09401775209
Product Details
M Ophthalmic devices
M1350 Keatoscope
Imported from abroad
Dates and Status
Apr 24, 2017
Apr 24, 2022
Cancellation Information
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